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FDA 510(k)

Flow-i 麻醉系統,Flow-c 麻醉系統,Flow-e 麻醉系統

K 號:K191027 · 2020-03-18

決定日期2020-03-18
產品代碼BSZ
諮詢委員會AN
決定相當於

器材摘要

Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System is the device name listed in this FDA 510(k) record. The listed applicant is Maquet Critical Care AB. It received FDA 510(k) clearance on 2020-03-18 under 510(k) number K191027. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?

Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System is a medical device that received FDA 510(k) clearance on 2020-03-18. The listed applicant is Maquet Critical Care AB. The 510(k) number is K191027.

When did Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System receive FDA 510(k) clearance?

Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System received FDA 510(k) clearance on 2020-03-18, under 510(k) number K191027.

Who is the listed applicant for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?

FDA 510(k) 記錄將 Maquet Critical Care AB 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System?

The FDA product code for Flow-i Anesthesia System, Flow-c Anesthesia System, Flow-e Anesthesia System is BSZ.

相關臨床試驗

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

其他以 Maquet Critical Care AB 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

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相關器械(代碼:BSZ)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

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